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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources January 28, 2025
Displaying entries 10051 - 10075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3910 lung adenocarcinoma HGNC:450 Homo sapiens (human) 60529 ALX4 direct assay evidence used in manual assertion
  • PMID:18978557
DOID:9744 type 1 diabetes mellitus HGNC:9951 Homo sapiens (human) 5967 REG1A direct assay evidence used in manual assertion
  • PMID:9564847
DOID:684 hepatocellular carcinoma HGNC:3688 Homo sapiens (human) 2260 FGFR1 direct assay evidence used in manual assertion
  • PMID:16452204
  • PMID:20155451
DOID:1681 heart septal defect HGNC:1078 Homo sapiens (human) 659 BMPR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21070126
DOID:0110414 retinitis pigmentosa 3 HGNC:29168 Homo sapiens (human) 23322 RPGRIP1L inference by association of genotype from phenotype used in manual assertion
  • PMID:22183348
DOID:1586 rheumatic fever HGNC:4187 Homo sapiens (human) 2638 GC inference by association of genotype from phenotype used in manual assertion
  • PMID:2737695
DOID:9976 heroin dependence HGNC:8153 Homo sapiens (human) 4985 OPRD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22500942
  • PMID:28692418
  • PMID:29173032
  • PMID:30171993
  • PMID:31907389
  • PMID:34031368
DOID:5844 myocardial infarction HGNC:7155 Homo sapiens (human) 4312 MMP1 direct assay evidence used in manual assertion
  • PMID:15009768
DOID:0050866 oral squamous cell carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B inference by association of genotype from phenotype used in manual assertion
  • PMID:21393552
DOID:684 hepatocellular carcinoma HGNC:1748 Homo sapiens (human) 999 CDH1 direct assay evidence used in manual assertion
  • PMID:30697077
DOID:1612 breast cancer HGNC:11364 Homo sapiens (human) 6774 STAT3 mutant phenotype evidence used in manual assertion
  • PMID:15374974
  • PMID:21740845
DOID:0111571 Weyers acrofacial dysostosis HGNC:19747 Homo sapiens (human) 132884 EVC2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:705 Leber hereditary optic neuropathy HGNC:7461 Homo sapiens (human) 4540 ND5 inference by association of genotype from phenotype used in manual assertion
  • PMID:16240359
  • PMID:16816025
  • PMID:1732158
  • PMID:19022198
  • PMID:21131053
DOID:0050328 congenital hypothyroidism HGNC:11040 Homo sapiens (human) 6528 SLC5A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:9171822
DOID:784 chronic kidney disease HGNC:4553 Homo sapiens (human) 2876 GPX1 direct assay evidence used in manual assertion
  • PMID:15954914
DOID:10024 migraine with aura HGNC:800 Homo sapiens (human) 477 ATP1A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12953268
DOID:77 gastrointestinal system disease HGNC:12663 Homo sapiens (human) 7412 VCAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11361181
DOID:2226 myeloproliferative neoplasm HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • PMID:12181402
DOID:0050547 familial medullary thyroid carcinoma HGNC:9967 Homo sapiens (human) 5979 RET inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3883 Lynch syndrome HGNC:7230 Homo sapiens (human) 4361 MRE11 inference by association of genotype from phenotype used in manual assertion
  • PMID:28218421
DOID:0070136 autosomal dominant cutis laxa 2 HGNC:3602 Homo sapiens (human) 10516 FBLN5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110654 long QT syndrome 13 HGNC:6266 Homo sapiens (human) 3762 KCNJ5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1070 primary open angle glaucoma HGNC:7610 Homo sapiens (human) 4653 MYOC mutant phenotype evidence used in manual assertion
  • PMID:23876925
DOID:2355 anemia HGNC:4922 Homo sapiens (human) 3098 HK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19651813
DOID:2841 asthma HGNC:7218 Homo sapiens (human) 4353 MPO inference by association of genotype from phenotype used in manual assertion
  • PMID:19544176
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025